Be at the heart of actionFly remote-controlled drones into enemy territory to gather vital information.

Apply Now

Head of Regulatory Affairs

Johnson & Johnson
High Wycombe
4 days ago
Create job alert

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com


Job Function: Regulatory Affairs Group


Job Sub Function: Regulatory Affairs


Job Category: People Leader


All Job Posting Locations: High Wycombe, Buckinghamshire, United Kingdom


Job Description

Are you ready to make a difference?


At Johnson & Johnson, we are committed to addressing and solving some of the most meaningful unmet medical needs through creating an environment where our employees feel valued and can reach their potential. This commitment is embedded in our Credo!


The Opportunity

An exciting new opportunity has arisen for a Head of Regulatory Affairs in the UK! In this role, you will develop short to long‑term business strategies, partner closely with EMEA team members, and achieve relevant patient outcomes, commercial, sales, and growth targets.


This includes developing the vision for and responsible for overall leadership and strategic direction of the Regulatory Affairs team to ensure licenses are obtained in a timely manner in line with business strategy and the business markets products with consistently high quality, safety and efficacy, minimising regulatory enforcement actions.



  • Developing and maintaining a deep understanding of the existing evolving regulatory environment and translating that to impactful regulatory strategies for our product portfolio
  • Ensuring regulatory and GMP compliance and inspection readiness at all times
  • Ensuring effective interaction and partnership with internal business stakeholders
  • Bringing thought leadership on innovative strategic approaches to drive the debate and deliver solutions that shape the regulatory framework
  • Ongoing development of regulatory team capabilities, retaining and attracting the best talent

Key Responsibilities
Regulatory Strategy & Leadership

  • Lead the UK Regulatory Affairs team, shaping strategy in alignment with UK portfolio, medical, and global priorities.
  • Provide strategic oversight for high‑quality submissions to the MHRA and ensure alignment with EMEA and local business goals.
  • Represent UK Regulatory Affairs in senior forums (e.g., G7 Heads of RA, Medical Leadership Teams), contributing insights and guidance.
  • Drive operational efficiency through process improvements, standardisation, and system enhancements.

Cross‑Functional Collaboration

  • Partner with internal teams (medical, marketing, sales, logistics, pricing) to ensure regulatory strategies support broader business objectives.
  • Ensure empowered regulatory representation at CVTs and collaborate across EMEA, Global, and ACCESS consortium countries to leverage synergies.

External Engagement

  • Develop and lead UK external stakeholder strategy, including strategic engagement with MHRA and other health authorities.
  • Influence national policy through ABPI working groups and Office for Life Sciences, in coordination with Health Affairs leadership.
  • Monitor and share regulatory trends across UK, Ireland, and EU, contributing to industry advocacy and policy shaping.

Operational Excellence

  • Support GRA‑EMEA initiatives and lead change management efforts to embed lessons learned and improve efficiency.
  • Collaborate on resource planning and manage the Regulatory Affairs budget effectively.

Qualifications
Education

  • Degree or equivalent experience in Pharmacy, Biology, Chemistry, or related Life Sciences.

Experience & Skills

  • Extensive strategic and operational Regulatory Affairs experience.
  • Solid understanding of UK, Ireland, and EU regulatory frameworks.
  • Familiarity with GMP, GDP, and QMS standards.
  • Proven leadership and team development capabilities.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.


We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.


Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center () or contact AskGS to be directed to your accommodation resource.


#J-18808-Ljbffr

Related Jobs

View all jobs

Head of Regulatory Affairs

Head of Regulatory Affairs

UK Head of Regulatory Affairs — Strategic Leader

UK Regulatory Affairs Leader: Strategy, Compliance & Impact

Associate Director, Regulatory Affairs

Regulatory Affairs Manager

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Neurodiversity in Medical Technology Careers: Turning Different Thinking into a Superpower

Medical technology sits at the intersection of health, engineering & innovation. From imaging & diagnostics to digital health apps, wearables & surgical robotics, medtech is about solving complex real-world problems that directly affect patients’ lives. To do that well, the sector needs people who think differently. If you live with ADHD, autism or dyslexia, you may have been told your brain is “too distracted”, “too literal” or “too disorganised” for a regulated, safety-critical industry. In reality, many traits that made school or previous jobs difficult can be huge strengths in medical technology – from pattern-spotting in clinical data to meticulous attention to detail in device testing. This guide is for neurodivergent job seekers exploring medical technology careers in the UK. We’ll cover: What neurodiversity means in a medtech context How ADHD, autism & dyslexia strengths map to common medtech roles Practical workplace adjustments you can ask for under UK law How to talk about your neurodivergence in applications & interviews By the end, you’ll have a clearer sense of where you might thrive in medical technology – & how to turn “different thinking” into a genuine superpower.

Medical Technology Hiring Trends 2026: What to Watch Out For (For Job Seekers & Recruiters)

As we move into 2026, the medical technology (MedTech) jobs market in the UK is changing fast. Hospitals and health systems are under pressure to do more with less. Diagnostics and devices are becoming smarter, more connected and more regulated. AI, robotics and remote monitoring are no longer “future tech” – they’re being built into mainstream care pathways. At the same time, budgets are tight, funding cycles are uneven and some healthtech start-ups are consolidating or being acquired. That means fewer vague “innovation” roles and more focus on medical technology jobs that directly support regulatory approval, patient safety, NHS adoption and commercial growth. Whether you are a MedTech job seeker planning your next move, or a recruiter building teams for medical device, diagnostics or digital health companies, this guide breaks down the key medical technology hiring trends for 2026.

Medical Technology Recruitment Trends 2025 (UK): What Job Seekers Need To Know About Today’s Hiring Process

Summary: UK medical technology hiring has shifted from title‑led CV screens to capability‑driven assessments that emphasise regulatory‑aware product delivery (QMS, ISO 13485), software lifecycle & risk (IEC 62304/14971), usability (IEC 62366), clinical & regulatory strategy (MDR/UKCA), device cyber security & privacy, and measurable patient/clinical and commercial impact. This guide explains what’s changed, what to expect in interviews & how to prepare—especially for SaMD engineers, AI/ML in medical devices, product & quality engineers, regulatory/clinical affairs specialists, validation/verification, manufacturing/operations, and digital health roles. Who this is for: Software/firmware engineers in medtech, SaMD/AI engineers, systems & verification engineers, quality & regulatory affairs (QARA), clinical evaluation/PMCF specialists, human factors engineers, medical device cyber security & privacy, test/validation, manufacturing & operations, field/service engineers, and medtech product managers in the UK.